74025-90-4

Usage

Properties

1. Chemical name: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium
2. Molecular structure: Complex molecular structure containing an amino group, a dihydropyrimidin-1-ium moiety, and a methoxycarbonyl group
3. Potential pharmaceutical applications: Structure suggests potential biological activity
4. Usage: May be used in drug development, as a research tool, or in chemical synthesis
5. Need for further research: Further studies needed to fully understand properties and potential uses

Specific content

Amino group
Dihydropyrimidin-1-ium moiety
Methoxycarbonyl group
Complex molecular structure
Potential pharmaceutical applications
Usage in drug development, research, or chemical synthesis
Need for further research to fully understand properties and potential uses

Upstream product

• 694-05-3 1,2,3,6-tetrahydropyridine 
• 86134-94-3 2-amino-6-(methoxycarbonyl)amino-4-(p-tolylsulfonyl)oxypyrimidine 1-oxide 
• 68020-77-9 methyl 5-<3,6-dihydro-1(2H)-pyridyl>-2-oxo-2H-<1,2,4>-oxadiazolo<2,3-a>pyrimidine-7-carbamate 
• 79-22-1 methyl chloroformate 
• 68020-78-0 2,6-diamino-4-(1,2,3,6-tetrahydro-1-pyridyl)pyrimidine 1-oxide 
• 68020-76-8 4-(1,2,3,6-tetrahydro-1-pyridyl)-2,6-bis(methoxycarbonylamino)-pyrimidine 1-oxide 
• 86134-93-2 methyl 2-amino-6-(p-tolylsulfonyl)oxy-4-pyrimidinecarbamate 
• 86134-92-1 methyl 2-amino-1,6-dihydro-6-oxo-4-pyrimidinecarbamate 
• 68020-80-4 N-cyanoacetyl-1,2,3,6-tetrahydropyridine 

Downstream Products

• 83395-28-2 butyl 7-<3,6-dihydro-1(2H)-pyridyl>-2H-<1,2,4>oxadiazolo<2,3-a>pyrimidine-5-carbamate 
• 86553-26-6 i-butyl 7-<3,6-dihydro-1(2H)-pyridyl>-2H-<1,2,4>oxadiazolo<2,3-a>pyrimidine-5-carbamate 
• 83395-25-9 methyl 7-<3,6-dihydro-1(2H)-pyridyl>-2-oxo-2H-<1,2,4>-oxadiazolo<2,3-c>pyrimidine-5-carbamate 

Relevant academic research and scientific papers

Pyrimidinecarbamate derivatives as intermediates

2,4-Disubstituted 6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxides of the formula STR1 wherein R1 is lower alkyl or lower alkoxy-lower alkyl, R2 is hydrogen or --COOR3 wherein R3 is lower alkyl or lower alkoxy-l

80. A New Route to the Synthesis of 2-Amino-6-(methoxycarbonyl)amino-4-(tetrahydropyridyl)pyrimidine 1-Oxide

A new approach to 2-amino-6-(methoxycarbonyl)amino-4-(1,2,3,6-tetrahydro-1-pyridyl)pyrimidine 1-oxide (3) is described.Methyl carbamate (5) reacted with guanidine to the pyrimidinecarbamate 6, which was successively

61. Synthesis of 2-Oxo-2H-oxadiazolo-pyrimidine-5-carbamates

Thermal cyclization of the pyrimidine-N-oxide dicarbamate 2 gives a 95:5 mixture of the 2-oxo-2H-oxadiazolo- and pyrimidinecarbamates 3 and 4.An efficient procedure for the conversion of 3 to 4, and vice versa, is described.

Process for the preparation of oxadiazolopyrimidine derivatives

A process for preparing oxadiazolopyrimidines of the formula STR1 wherein R is alkyl or alkoxyalkyl, by reacting a compound of the formula STR2 wherein R is as set forth above, with phosgene, is described.